Polymerization inhibitor of diacetylene



PQLYli/IERIZATION lTOR F DIACETYLENE No Drawing. Application October 26, 1953, Serial No. 388,459

4 Claims. (Cl. 252-1) This invention relates to the inhibition of polymerization. In one embodiment, it pertains to the inhibition of undesirable polymer growth in processing aquipment. Specifically, it is concerned with a method for the stabilization of diacetylene, or of mixtures containing diacetylene, against polymerization and the stabilized compositions so produced.

If acetylene is produced from hydrocarbons, e. g., by the well known electric arc process or by thermal decomposition or dissociation, the acetylene-containing gas mixture produced generally contains diacetylene as well, in amounts ranging from as little as 0.05% to as much as The purification of such an acetylenic gas mixture is usually accomplished by the selective action of suitable solvents. A great number and variety of solvents have been proposed and are efiectively employed in well-developed purification processes. However, in these conventional methods of absorption andv stripping, the gas mixture is exposed to conditions of temperature and pressure under which some of the diacetylene present polymerizes, and provision must be made in all such processes for periodic removal of the diacetylene polymers to prevent their excessive build-up in the solvent in the absorption step. This requires additional, specialized filtration equipment as well as added process steps which are costly with regard to both time and capital expense. Frequently, too, the diacetylene polymer collects in the less accessible parts of the system, fouling up equipment lines, columns, and the like. Usually, this particular polymer is of such a small particle size that it plugs the filter used for separating it, so that only a small amount can be filtered in each operation and an inordinate length of time is required to wring the filter cake dry.

Methods have been proposed for removal of diacetylene from the gas stream, but these are cumbersome and expensive since they require additional process steps prior to the usual solvent purification operation which utilizes special equipment and significant quantities of special chemicals for treating purposes.

it is an object of the present invention, therefore, to provide a method whereby undesirable polymer growth in the solvent purification of acetylene is inhibited.

It is a further object of the invention to provide a method for stabilization of diacetylene against polymerization.

It is a still further object of the invention to provide novel stabilized compositions comprising diacetylene, a solvent therefor, and an added polymerization inhibitor which do not polymerize when subjected to conditions under which such compositions lacking the inhibitor polymerize readily and rapidly. Other objects and advantages of the invention will be apparent from the following description and the appended claims.

According to the invention, diacetylene contained in a solvent is stabilized against polymerization by the addition thereto of small quantities of hexamethylene tetramine. The composition comprising diacetylene, a

2,715,1fi4 Patented Aug. 9, 1955 solvent therefor, and a minor amount of hexamethylene tetramine will not exhibit any significant polymer formation on prolonged periods of storage or when subjected to the temperatures commonly encountered in solvent purification systems for acetylene purification.

The following example illustrates the invention but is not to be construed as limiting it in any manner.

EXAMPLE I Diacetylene was generated by dropping 40% sodium hydroxide into a well-stirred solution of 1,4-dichlorobutyne in ethanol at a temperature of approximately C. The product gas was passed through Dry Ice traps and then allowed to bubble through a fritted gas bubbler into technical-grade butyrolactone at room temperature to make a stock solution of 0.3 g. of diacetylene per milliliter of solution. In the polymerization tests, 20 ml. of a test mixture containing a known amount of the diacetylene stock solution, butyrolactone, water, and a weighed amount of the inhibitor were introduced into a thick-walled test tube. The mixture was frozen and the end of the test tube was drawn oil in a torch flame to make a sealed ampoule. The sealed ampoules were wrapped in bronze screen and placed in an oven maintained at 125 C. for 16 hours, after which they were removed and inspected for polymer content. Blanks were run in which only butyrolactone and mixtures of butyrolactone, water and dracetyleue were present. Results of a series of such tests are presented in Table I Table I Test No Test Mixture Condition of Test Mixture 1 50% Butyrolactone50%HzO Usual straw color; perfectly clear; unchanged. Same as in Test N o. 1 above Clear, pale yellow solution.

plus 1.0% hexamethylene tetramine.

3 50% BLf-50% H20 plus Reddish brown suspension of 0.25% dracetylene. polymer; fairly heavy ppt. of finely divided material.

4 Same as 111 Test No. 3 above Some reddish brown polymer plus 0.01% hexamethylene in suspension; smaller tetramine. amount of finely divided ppt. than in 3 above.

5 Same as rn Test N o. 3 above Deep red wine color; no visplus 0.1% hexamethylene ible ppt. tetramine.

6 Same as in Test No. 3 above Clear, ember-colored soluplus 1.0% hexamethylene tion; no ppt. tetramine.

7 50% BI .50% H2O plus Heavy brown ppt. settled 0.5% dlacetylene. on bottom of tube; liquid also full of suspended polymer.

8 Same as in Test N o. 7 above Brown suspension; finely plus 0.1% hexamethylene divided precipitate. tetramine.

9 Same as in Test No. 7 above Dark amber-colored, clear plus 0.5% hexamethylene solution; no solid at all evitetramine. dent.

10 10% BLQ0% H2O plus 0.5% Perfectly clear, water White hexamethylene tetramine. solution.

11 10% BL- H2O plus Rich tan colored suspension;

0.25% dracetylene. fairly heavy semi-coagu- I lated precipitate.

l2 Same as 111 Test N o. 11 above Light amber color, slight plus 0.1% hexamethylene green fluorescence; only tetramine. trace of polymer film on surface of liquid.

13 Same as in Test No. 11 above Pale yellow, perfectly clear;

plus 0.5% hexamethylene only slight trace of fluorestetramine. cence.

*Bntyrolaetone.

ramine.

thereof.

pends somewhat on the amount of diacetylene present and the degree of inhibition desired. In general, only minor quantities of the inhibitor are required. Concentrations in the range of about 0.01% to about 5% by weight of the total composition are suitable, with con centrations from about 0.1% to about 1% being preferred. The stabilizing agent may, of course, be employed in as great a concentration as desired.

The inhibitor of the invention is not restricted to use with butyrolactone as set out in the example above. Hexamethylene tetramine may be used to inhibit the polymerization of diacetylene in other organic solvents such as acetonyl acetone, dioxane, dimethyl formamide, and the like. In solvent systems where such solvents are used to absorb acetylene from a gas stream containing it in combination with other gases including diacetylene, polymerization of the diacetylene is effectively inhibited by the presence of a minor amount of hexamethylene tetramine. To inhibit polymer formation during the absorption-stripping operation, the inhibitor can be added directly to the solvent feed stream, or it may be introduced as a solution of the desired concentration at some point in the absorption system. The inhibiting power of the hexamethylene tetramine is not affected by continual reuse; hence, recirculation of the solvent provides as effective inhibition as the introduction of the fresh solution.

The inhibitor of the invention may also be utilized for preparing stabilized compositions of diacetylene in a solvent which can be safely stored over a period of time without undergoing polymerization with its usual attendant hazards.

The term consisting essentially of which appears in the claims hereof is intended to refer to a composition in which the total amounts of the components set forth in the claims constitute the predominant proportion in the composition. Such term is not intended to exclude the presence of materials such as moisture or water or other material which may be present as an inert diluent and does not adversely affect the solution in any manner. However, the term is intended to exclude the presence of materials which so change the character of the composition that it can no longer be regarded as a solution of diacetylene.

What is claimed is:

1. A composition of matter consisting essentially of diacetylene, a solvent therefor, and hexamethylene tetramine in an amount from about 0.01% to about 5% by weight of the total composition.

2. A composition of matter consisting essentially of diacetylene, a solvent therefor, and hexamethylene tetramine in an amount from about 0.1% to about 1% by Weight of the total composition.

3. A composition of matter consisting essentially of diacetylene, butyrolactone, and hexamethylene tetramine in an amount from about 0.01% to about 5% by weight of the total composition.

4. A composition of matter consisting essentially of diacetylene, butyrolactone and hexarnethylene tetramine in an amount from about 0.1% to about 1% by weight of the total composition.

References Cited in the file of this patent UNITED STATES PATENTS 2,601,673 McMillan et al. June 24, 1952 

1. A COMPOSITION OF MATTER CONSISTING ESSENTIALLY OF DIACETYLENE, A SOLVENT THEREFOR, AND HEXAMETHYLENE TETRAMINE IN AN AMOUNT FROM ABOUT 0.01% TO ABOUT 5% BY WEIGHT OF THE TOTAL COMPSOITION. 